Taiwan FDA registration fbd3519e6fa75d275ed263449a567cb4
“Meditech”MICROVENT RESUSCITATOR
TW: “美迪泰克”氣動力式緊急呼吸器
Taiwan·Risk Class 2·MD·B.N.O.S. Meditech Limited·Registered Mar 10, 2022 – Mar 10, 2027ActiveRegistration details
- Analysis ID
- fbd3519e6fa75d275ed263449a567cb4
- License Form
- Ministry of Health Medical Device Import No. 035322
- Customs Code
- DHA05603532205
Company information
- Manufacturer
- B.N.O.S. Meditech Limited
- Manufacturer Country
- United Kingdom
- Authorized Representative
- EMSTREAM CORPORATION
Product details
- Intended Use
- Details are as detailed as approved Chinese instructions
- Product Type (Level 1)
- D Anesthesiology
- Product Type (Level 2)
- D5925 Powered Emergency Respirator
- Import Information
- Imported from abroad
Dates and status
- Registration Date
- Mar 10, 2022
- Expiry Date
- Mar 10, 2027
About this record
Access comprehensive regulatory information for “Meditech”MICROVENT RESUSCITATOR in Taiwan's medical device market through Pure Global AI's free database. This Risk Class 2 medical device is registered under number fbd3519e6fa75d275ed263449a567cb4 and manufactured by B.N.O.S. Meditech Limited. The authorized representative in Taiwan is EMSTREAM CORPORATION.
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